510(k) K113616 ยท KGI Densitometer, Bone
ACCUDXA2
| Applicant | Lone Oak Medical Technologies, LLC, Doylestown PA, US |
| Decision | Substantially Equivalent, Apr 27, 2012 |
| Received | Dec 7, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113616
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.